ARE PROSTAGLANDINS INVOLVED IN THE RESTITUTION OF AN OXALATE- DAMAGED EPITHELIUM?

C.I. CASALI; MOREL GOMEZ, EMANUEL; ERJAVEC, LUCIANA; PARRA LEANDRO; DEL CARMEN FERNÁNDEZ, MARÍA

MENDOZA

Congreso; LVIII Reunión de la Sociedad Argentina de Investigaciones Bioquímicas y Biología Molecular- SAIB 2022? 8 al 11 de Noviembre de 2022, Ciudad de Mendoza, Argentina.; 2022

SAIB

LI-P04-83ARE PROSTAGLANDINS INVOLVED IN THE RESTITUTION OF AN OXALATE- DAMAGED EPITHELIUM?Casali CI 1,2, Morel Gómez ED 1, Erjavec LC 1,2, Parra LG 1,2, Marino JI 1, Fernández-Tomé MC 1,2.1Universidad de Buenos Aires, Facultad de Farmacia y Bioquímica-Biología Celular y Molecular. 2 IQUIFIB-Alejandro Paladini -UBA-CONICET.E-mail: ccasali@ffyb.uba.ar.Instituto DrRenal collecting ducts, which are involved in the urine concentration mechanism, are immersed in an extracellular matrix with the highest body osmolarity. This hyperosmolarity is a key signal for renal cell differentiation and for the establishment of the urine concentration mechanism. However, hyperosmolarity can induce cell death when there is a great osmolarity change. Renal cells activate adaptive and protective mechanisms to survive in the hyperosmolar environment. One important cell mechanism is the expression of osmoprotective genes such as cyclooxygenase 2 (COX2). Moreover, renal ducts are exposed to wastes coming from blood filtration that include nephrotoxic drugs and kidney stones. Calcium oxalate stones are the most common type of kidney stone. Crystal aggregates are harmful for epithelial renal cells and tubular structures, and the damage could lead to renal kidney disease. Our prior results showed that oxalate modulates COX2 mRNA and protein expression in renal differentiated epithelial cells, but the role of this protein is still unknown. The aim of the present work is to evaluate whether prostaglandins, the COX2 products, are involved in the regeneration mechanism of differentiated renal epithelial cells damaged with oxalate. To do that, renal epithelial cells MDCK were grown in a hyperosmolar environment (512 mOsm/Kg H2O) for 72 h to get a differentiated epithelium and then subjected to 1.5 mM oxalate (Ox) for 24, 48 and 72 h. To inhibit COX2, 10 μM NS398 was added 30 min before Ox treatment; and to restore the inhibition, PGE2 (10-5, 10-6 and 10-7 M) was added 30 min after Ox addition. After treatment, cells were harvested, counted and cell viability was determined. Cell morphology and COX2 expression was also evaluated. Cells treated with 24 h of Ox showed a spindle-shaped morphology characteristic of an epithelial mesenchymal transition (EMT) and NS398 addition before Ox treatment did not allow these EMT. After 48 h of Ox cells started to recover their typical epithelial morphology. Cell treated with NS398 before Ox showed a cobblestone morphology, but gaps in the monolayer were observed. Control conditions showed the typical epithelial cobblestone morphology after 24 and 48 h. PGE2 addition to cells treated with NS398 and Ox did not allow the EMT at 24 and 48h. Moreover, PGE2 treated cells showed a morphology characteristic of an epithelial cells (cobblestone). Ox decreased the number of cells at 24 h and 48 h compared to controls. The treatment with NS398 before Ox addition caused a slight decrease of cell numbers at 24 h but not at 48 h. PGE2 addition did not affect cell number at 24 and 48 h. Cell viability did not change after all treatments. NS398 induced COX2 expression and the addition of PGE2 slightly decreased it. The results showed that PGE2 may be implicated in the restitution of the differentiated epithelia damaged with oxalate, but furtherexperiments are needed to elucidate the molecular mechanisms involved.